Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1442638생성일: 2026년 10월 27일
Potassium methyl N-cyanodithioimidocarbonate → 3-(4-Amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl ester
https://huagongshe.com/reaction/1442638
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium methyl N-cyanodithioimidocarbonate | HCID 2733091 | — |
| 반응물 | 4-Chloro-2-cyano-3-hydroxy-but-2-enoic acid tert-butyl ester | HCID 76837579 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 3-(4-Amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl ester | HCID 68540342 | — |
반응 단계
To a stirred solution of 4-chloro-2-cyano-3-hydroxy-but-2-enoic acid tert-butyl ester Compound 1c (51.3 g, 236 mmol) at 0° C. in acetone (750 mL) was added potassium methyl N-cyanodithioimidocarbonate Compound 1e (40.2 g, 236 mmol). After 1 hr the reaction was allowed to warm to RT. The reaction mixture was evaporated down after stirring for 18 hrs. The resulting residue was extracted with ethyl acetate from saturated NaHCO3. The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure to yield a tan foam, 3-(4-amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl ester Compound 1h, 72.2 g. 1H NMR (CDCl3) δ 4.34 (br s, 2H), 3.14 (br s, 1H), 2.70 (br s, 3H), 1.47 (br s, 9H). MS 314 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07659284B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-8aafb594f24d4c63800e65f8ca8aeeb0 |
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| 출처 메모 | uspto-grants-2010_02 |
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